Detalhe da pesquisa
1.
Mild Chronic Colitis Triggers Parkinsonism in LRRK2 Mutant Mice Through Activating TNF-α Pathway.
Mov Disord
; 37(4): 745-757, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34918781
2.
Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48).
J Biomed Sci
; 28(1): 65, 2021 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34565360
3.
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.
Brain
; 143(11): 3352-3373, 2020 12 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33141179
4.
Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: case series and literature review.
BMC Neurol
; 20(1): 101, 2020 Mar 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32183746
5.
Altered gut microbiota and inflammatory cytokine responses in patients with Parkinson's disease.
J Neuroinflammation
; 16(1): 129, 2019 Jun 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31248424
6.
Reply to: Mild Chronic Colitis Triggers Parkinsonism in LRRK2 Mutant Mice through Activating TNF-α Pathway.
Mov Disord
; 37(3): 665-666, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35092086
7.
A low-carbohydrate/high-fat diet reduces blood pressure in spontaneously hypertensive rats without deleterious changes in insulin resistance.
Am J Physiol Heart Circ Physiol
; 304(12): H1733-42, 2013 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23604708
8.
Neuroinflammation Upregulated Neuronal Toll-Like Receptors 2 and 4 to Drive Synucleinopathy in Neurodegeneration.
Front Pharmacol
; 13: 845930, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35401198
9.
Endocrine and Growth Disorders in Taiwanese Children With 22q11.2 Deletion Syndrome.
Front Endocrinol (Lausanne)
; 13: 771100, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35432203
10.
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 gene.
Stem Cell Res
; 51: 102190, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33517123
11.
UQCRC1 engages cytochrome c for neuronal apoptotic cell death.
Cell Rep
; 36(12): 109729, 2021 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34551295
12.
In vitro genome editing rescues parkinsonism phenotypes in induced pluripotent stem cells-derived dopaminergic neurons carrying LRRK2 p.G2019S mutation.
Stem Cell Res Ther
; 12(1): 508, 2021 09 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34551822
13.
Reprogramming of a human induced pluripotent stem cell (iPSC) line from a patient with neurodegeneration with brain iron accumulation (NBIA) harboring a novel frameshift mutation in C19orf12 gene.
Stem Cell Res
; 49: 102032, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33068888
14.
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-057-05) from a patient with familial parkinsonism and polyneuropathy having a heterozygous p.Y314S mutation in UQCRC1 gene.
Stem Cell Res
; 49: 102031, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33070102
15.
A dual inhibitor targeting HMG-CoA reductase and histone deacetylase mitigates neurite degeneration in LRRK2-G2019S parkinsonism.
Aging (Albany NY)
; 12(24): 25581-25598, 2020 11 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33231564
16.
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-048-05) from a patient with ALS and parkinsonism having a hexanucleotide repeat expansion mutation in C9orf72 gene.
Stem Cell Res
; 44: 101734, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32151952
17.
Genetic analysis of PODXL gene in patients with familial and young-onset Parkinson's disease in a Taiwanese population.
Neurobiol Aging
; 84: 235.e9-235.e10, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31564376
18.
Mammalian target of rapamycin is a critical regulator of cardiac hypertrophy in spontaneously hypertensive rats.
Hypertension
; 54(6): 1321-7, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19884565